Digestive Disease Center, Bispebjerg Hospital, 2400 Copenhagen, Denmark.
Wellcome Centre for Cell-Matrix Research, Division of Cell Matrix and Regenerative Medicine, Faculty of Biology Medicine and Health, University of Manchester, Manchester M16 8FB, UK.
Int J Mol Sci. 2020 Mar 10;21(5):1887. doi: 10.3390/ijms21051887.
Mucosal healing determined by endoscopy is currently the remission standard for ulcerative colitis (UC). However, new criteria for remission are emerging, such as histologic normalization, which appears to correlate better to the risk of relapse. Here, we study mucosal healing on a molecular and functional level in quiescent UC. We obtained endoscopic biopsies from 33 quiescent UC patients and from 17 controls. Histology was assessed using Geboes score. Protein and mRNA levels were evaluated for the tight junction proteins claudin-2, claudin-4, occludin, and tricellulin, as well as Cl/HCO exchanger DRA, and cyclo-oxygenase enzymes (COX-1, COX-2). The mucosal activity of COX-1 and COX-2 enzymes was assessed in modified Ussing chambers, measuring electrogenic ion transport (short-circuit current, SCC). Chronic inflammation was present in most UC patients. The protein level of claudin-4 was reduced, while mRNA-levels of claudin-2 and claudin-4 were upregulated in UC patients. Surprisingly, the mRNA level of COX-1 was downregulated, but was unaltered for COX-2. Basal ion transport was not affected, while COX-2 inhibition induced a two-fold larger decrease in SCC in UC patients. Despite being in clinical and endoscopic remission, quiescent UC patients demonstrated abnormal mucosal barrier properties at the molecular and functional level. Further exploration of mucosal molecular signature for revision of current remission standards should be considered.
内镜下确定的黏膜愈合目前是溃疡性结肠炎(UC)的缓解标准。然而,新的缓解标准正在出现,如组织学正常化,这似乎与复发风险相关性更好。在这里,我们研究了处于缓解期的 UC 在分子和功能水平上的黏膜愈合。我们从 33 例处于缓解期的 UC 患者和 17 例对照者中获得了内镜活检。采用 Geboes 评分评估组织学。评估紧密连接蛋白 claudin-2、claudin-4、occludin 和 tricellulin,以及 Cl/HCO 交换器 DRA 和环氧化酶(COX-1、COX-2)的蛋白和 mRNA 水平。在改良的 Ussing 室中评估 COX-1 和 COX-2 酶的黏膜活性,测量电化学离子转运(短路电流,SCC)。大多数 UC 患者存在慢性炎症。claudin-4 的蛋白水平降低,而 claudin-2 和 claudin-4 的 mRNA 水平在 UC 患者中上调。令人惊讶的是,COX-1 的 mRNA 水平下调,但 COX-2 没有改变。基础离子转运不受影响,而 COX-2 抑制在 UC 患者中诱导 SCC 减少两倍。尽管处于临床和内镜缓解期,处于缓解期的 UC 患者在分子和功能水平上表现出异常的黏膜屏障特性。应考虑进一步探索黏膜分子特征,以修订当前的缓解标准。